Disease: Autism Spectrum Disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs370911031
NCS1
0.925 0.040 9 130219801 missense variant G/A snv 1.5E-04 8.4E-05 2
rs3735653
EN2
0.925 0.040 7 155458738 missense variant C/G;T snv 0.54 2
rs3747333
NLGN4X
0.925 0.040 X 5893491 missense variant G/A;C;T snv 7.6E-03 3
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs7170637
CYFIP1
0.925 0.040 15 22903836 missense variant C/T snv 0.18 0.30 2
rs73598374
ADA
0.790 0.280 20 44651586 missense variant C/A;G;T snv 7.1E-06; 6.2E-02 8
rs747756965
DNAH8
0.925 0.040 6 38775924 missense variant T/A;C snv 4.0E-06 2
rs751945904
NLGN4X
0.925 0.040 X 5893158 missense variant G/A snv 1.1E-05 2
rs768913131
NRXN1
0.925 0.040 2 50552821 missense variant G/A snv 3
rs79667838
GRPR
0.882 0.120 X 16150432 missense variant C/T snv 3.0E-04 4.8E-04 3
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 13
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs1340513
KDM4C
0.882 0.120 9 6977633 intron variant G/A snv 0.75 4
rs167771
DRD3
0.827 0.280 3 114157428 intron variant G/A;T snv 5
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs1861972
EN2
0.925 0.040 7 155461298 intron variant G/A snv 0.72 2
rs1861973
EN2
0.925 0.040 7 155461450 intron variant T/C snv 0.73 2
rs1881084
SND1
0.925 0.040 7 127704626 intron variant G/A snv 0.33 2
rs1912960
GABRA4
0.925 0.040 4 46951864 intron variant G/C snv 0.28 2